Vargas Celibell Y, Wang Liqun, Castellanos de Belliard Yaritza, Morban Maria, Diaz Hilbania, Larson Elaine L, LaRussa Philip, Saiman Lisa, Stockwell Melissa S
Department of Pediatrics, Columbia University, New York, NY, USA.
School of Nursing, Columbia University, New York, NY, USA; Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA.
Clin Epidemiol. 2016 Jan 6;8:1-5. doi: 10.2147/CLEP.S95847. eCollection 2016.
To assess the feasibility and validity of unsupervised participant-collected nasal swabs to detect respiratory pathogens in a low-income, urban minority population.
This project was conducted as part of an ongoing community-based surveillance study in New York City to identify viral etiologies of acute respiratory infection. In January 2014, following sample collection by trained research assistants, participants with acute respiratory infection from 30 households subsequently collected and returned a self-collected/parent-collected nasal swab via mail. Self/parental swabs corresponding with positive reverse transcription polymerase chain reaction primary research samples were analyzed.
Nearly all (96.8%, n=30/31) households agreed to participate; 100% reported returning the sample and 29 were received (median time: 8 days). Most (18; 62.1%) of the primary research samples were positive. For eight influenza-positive research samples, seven (87.5%) self-swabs were also positive. For ten other respiratory pathogen-positive research samples, eight (80.0%) self-swabs were positive. Sensitivity of self-swabs for any respiratory pathogen was 83.3% and 87.5% for influenza, and specificity for both was 100%. There was no relationship between level of education and concordance of results between positive research samples and their matching participant swab.
In this pilot study, self-swabbing was feasible and valid in a low-income, urban minority population.
评估在低收入城市少数族裔人群中,由参与者自行采集鼻拭子检测呼吸道病原体的可行性和有效性。
本项目是纽约市一项正在进行的基于社区的监测研究的一部分,旨在确定急性呼吸道感染的病毒病因。2014年1月,在经过培训的研究助理采集样本后,来自30个家庭的急性呼吸道感染参与者随后通过邮件自行采集并返回了鼻拭子。对与逆转录聚合酶链反应初步研究样本阳性结果相对应的自我/家长采集的拭子进行了分析。
几乎所有(96.8%,n=30/31)家庭同意参与;100%报告已返回样本,收到29份(中位时间:8天)。大多数(18份;62.1%)初步研究样本呈阳性。对于8份流感阳性研究样本,7份(87.5%)自我采集的拭子也呈阳性。对于其他10份呼吸道病原体阳性研究样本,8份(80.0%)自我采集的拭子呈阳性。自我采集拭子对任何呼吸道病原体的敏感性为83.3%,对流感的敏感性为87.5%,两者的特异性均为100%。教育程度与阳性研究样本及其匹配的参与者拭子之间的结果一致性无关。
在这项试点研究中,自我采集拭子在低收入城市少数族裔人群中是可行且有效的。